Cleared Traditional

K031990 - ELECSYS PRECICONTROL TROPONIN T

K031990 is the FDA 510(k) clearance for ELECSYS PRECICONTROL TROPONIN T by Roche Diagnostics Corp.. It is a Class 1 Toxicology device (product code JJX) cleared through the Traditional 510(k) pathway after a 54-day FDA review.

K031990 · Roche Diagnostics Corp. · Toxicology device
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Aug 2003
Decision
54d
Days
Class 1
Risk

K031990 is an FDA 510(k) clearance for the ELECSYS PRECICONTROL TROPONIN T. Classified as Single (specified) Analyte Controls (assayed And Unassayed) (product code JJX), Class I - General Controls.

Submitted by Roche Diagnostics Corp. (Indianapolis, US). The FDA issued a Cleared decision on August 20, 2003 after a review of 54 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.1660 - the FDA toxicology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Roche Diagnostics Corp. devices

Submission Details

510(k) Number K031990 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 27, 2003
Decision Date August 20, 2003
Days to Decision 54 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
33d faster than avg
Panel avg: 87d · This submission: 54d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJX Single (specified) Analyte Controls (assayed And Unassayed)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1660
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - JJX Single (specified) Analyte Controls (assayed And Unassayed)

All 268
Devices cleared under the same product code (JJX) and FDA review panel - the closest regulatory comparables to K031990.
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ELECYS SHBG CALCHECK
K031698 · Roche Diagnostics Corp. · Aug 2003
MAS BILIRUBIN LIQUID ASSAYED BILIRUBIN CONTROL
K031890 · Medical Analysis Systems, Inc. · Jul 2003
SAS RSV CONTROL KIT
K030628 · Sa Scientific, Inc. · Mar 2003
WAKO NEFA LINEARITY SET
K030065 · Wako Chemicals USA, Inc. · Feb 2003